Cilengitide hydrochloride

(Synonyms: EMD 121974 hydrochloride)
71 Cited Publications
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Based on 71 publication(s) in Google Scholar

Cilengitide hydrochloride (EMD 121974 hydrochloride) is an integrin (integrin) inhibitor with blood-brain barrier permeability, with IC50 values against human targets as follows: 0.61 nM for αvβ3, 8.4 nM for αvβ5, 14.9 nM for α5β1, 5400 nM for αIIbβ3, 2050 nM for αvβ6, 2350 nM for αvβ8. Cilengitide hydrochloride inhibits the binding of integrins to vitronectin, fibronectin, fibrinogen and LAP (TGF-β), and serves as an internal standard for solid-phase integrin binding assays. Cilengitide hydrochloride inhibits tumor cell viability, induces apoptosis, reduces the phosphorylation levels of STAT3, AKT and mTOR, downregulates the expression of PD-L1, inhibits cell viability and angiogenesis, regulates anti-tumor immune responses and slows tumor growth. Cilengitide hydrochloride can be used in research related to glioblastoma, melanoma, advanced solid tumors and refractory brain tumors.

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  • CAS. Nr.: 188969-00-8
  • Formel: C27H41ClN8O7
  • Molecular Weight:625.12
  • Speicherung:

    Please store the product under the recommended conditions in the Certificate of Analysis.

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Cell Proliferation/Viability AssayIFIHCWB
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  • Cell Proliferation/Viability Assay
  • IF

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